The following data is part of a premarket notification filed by Intl. Immunoassay Laboratories, Inc. with the FDA for Proposed New Use Of Instrument System And Test Kit.
Device ID | K912231 |
510k Number | K912231 |
Device Name: | PROPOSED NEW USE OF INSTRUMENT SYSTEM AND TEST KIT |
Classification | U.v. Method, Cpk Isoenzymes |
Applicant | INTL. IMMUNOASSAY LABORATORIES, INC. 1900 WYATT DR., #11 Santa Clara, CA 95054 |
Contact | Vipin D Shah |
Correspondent | Vipin D Shah INTL. IMMUNOASSAY LABORATORIES, INC. 1900 WYATT DR., #11 Santa Clara, CA 95054 |
Product Code | JHW |
CFR Regulation Number | 862.1215 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-05-20 |
Decision Date | 1991-07-08 |